Real-world evidence of adjuvant gemcitabine plus capecitabine vs gemcitabine monotherapy for pancreatic ductal adenocarcinoma.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
15 05 2022
Historique:
revised: 12 11 2021
received: 30 08 2021
accepted: 02 12 2021
pubmed: 23 12 2021
medline: 29 4 2022
entrez: 22 12 2021
Statut: ppublish

Résumé

The added value of capecitabine to adjuvant gemcitabine monotherapy (GEM) in pancreatic ductal adenocarcinoma (PDAC) was shown by the ESPAC-4 trial. Real-world data on the effectiveness of gemcitabine plus capecitabine (GEMCAP), in patients ineligible for mFOLFIRINOX, are lacking. Our study assessed whether adjuvant GEMCAP is superior to GEM in a nationwide cohort. Patients treated with adjuvant GEMCAP or GEM after resection of PDAC without preoperative treatment were identified from The Netherlands Cancer Registry (2015-2019). The primary outcome was overall survival (OS), measured from start of chemotherapy. The treatment effect of GEMCAP vs GEM was adjusted for sex, age, performance status, tumor size, lymph node involvement, resection margin and tumor differentiation in a multivariable Cox regression analysis. Secondary outcome was the percentage of patients who completed the planned six adjuvant treatment cycles. Overall, 778 patients were included, of whom 21.1% received GEMCAP and 78.9% received GEM. The median OS was 31.4 months (95% CI 26.8-40.7) for GEMCAP and 22.1 months (95% CI 20.6-25.0) for GEM (HR: 0.71, 95% CI 0.56-0.90; logrank P = .004). After adjustment for prognostic factors, survival remained superior for patients treated with GEMCAP (HR: 0.73, 95% CI 0.57-0.92, logrank P = .009). Survival with GEMCAP was superior to GEM in most subgroups of prognostic factors. Adjuvant chemotherapy was completed in 69.5% of the patients treated with GEMCAP and 62.7% with GEM (P = .11). In this nationwide cohort of patients with PDAC, adjuvant GEMCAP was associated with superior survival as compared to GEM monotherapy and number of cycles was similar.

Identifiants

pubmed: 34935139
doi: 10.1002/ijc.33916
pmc: PMC9303436
doi:

Substances chimiques

Deoxycytidine 0W860991D6
Capecitabine 6804DJ8Z9U
Gemcitabine 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1654-1663

Informations de copyright

© 2021 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.

Références

J Natl Compr Canc Netw. 2017 Aug;15(8):1028-1061
pubmed: 28784865
CA Cancer J Clin. 2018 Jan;68(1):7-30
pubmed: 29313949
J Clin Oncol. 2007 Jun 1;25(16):2212-7
pubmed: 17538165
Ann Oncol. 2015 Sep;26 Suppl 5:v56-68
pubmed: 26314780
BMC Cancer. 2021 Mar 23;21(1):300
pubmed: 33757440
Ann Surg. 2022 Apr 1;275(4):769-775
pubmed: 32773631
JAMA. 2007 Jan 17;297(3):267-77
pubmed: 17227978
N Engl J Med. 2013 Oct 31;369(18):1691-703
pubmed: 24131140
Br J Surg. 2015 Jun;102(7):746-54
pubmed: 25833230
Curr Mol Med. 2013 Mar;13(3):340-51
pubmed: 23331006
N Engl J Med. 2014 Sep 11;371(11):1039-49
pubmed: 25207767
Br J Cancer. 2009 Sep 15;101(6):908-15
pubmed: 19690548
World J Oncol. 2019 Feb;10(1):10-27
pubmed: 30834048
Cancer. 1993 Oct 1;72(7):2118-23
pubmed: 8104092
Lancet. 2017 Mar 11;389(10073):1011-1024
pubmed: 28129987
N Engl J Med. 2011 May 12;364(19):1817-25
pubmed: 21561347
J Chronic Dis. 1987;40(5):373-83
pubmed: 3558716
JAMA Surg. 2019 Nov 1;154(11):1038-1048
pubmed: 31483448
Ann Surg. 2020 Apr;271(4):e102-e104
pubmed: 32084037
Int J Cancer. 2022 May 15;150(10):1654-1663
pubmed: 34935139
J Clin Oncol. 2009 Nov 20;27(33):5513-8
pubmed: 19858379
Eur J Cancer. 2020 Jan;125:83-93
pubmed: 31841792
J Clin Oncol. 2016 Jul 20;34(21):2541-56
pubmed: 27247221
Lancet. 2016 Jul 16;388(10041):248-57
pubmed: 27265347
N Engl J Med. 2018 Dec 20;379(25):2395-2406
pubmed: 30575490
J Clin Oncol. 2019 Aug 10;37(23):2082-2088
pubmed: 31180816

Auteurs

Evelien J M de Jong (EJM)

Department of Internal Medicine, Division of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center+, Maastricht, The Netherlands.

Quisette P Janssen (QP)

Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Tessa F A Simons (TFA)

Department of Internal Medicine, Division of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center+, Maastricht, The Netherlands.

Marc G Besselink (MG)

Department of Surgery, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Bert A Bonsing (BA)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.

Stefan A W Bouwense (SAW)

Department of Surgery, Maastricht University Medical Center+, Maastricht, The Netherlands.

Sandra M E Geurts (SME)

Department of Internal Medicine, Division of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center+, Maastricht, The Netherlands.

Marjolein Y V Homs (MYV)

Department of Medical Oncology, Erasmus Medical Center, Rotterdam, The Netherlands.

Vincent E de Meijer (VE)

Department of Surgery, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands.

Vivianne C G Tjan-Heijnen (VCG)

Department of Internal Medicine, Division of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center+, Maastricht, The Netherlands.

Hanneke W M van Laarhoven (HWM)

Department of Medical Oncology, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Liselot B J Valkenburg-van Iersel (LBJ)

Department of Internal Medicine, Division of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center+, Maastricht, The Netherlands.

Johanna W Wilmink (JW)

Department of Medical Oncology, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Lydia G van der Geest (LG)

Department of Research, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands.

Bas Groot Koerkamp (BG)

Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Judith de Vos-Geelen (J)

Department of Internal Medicine, Division of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht University Medical Center+, Maastricht, The Netherlands.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH